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Moxi Rolls (ny)

FDA UDI

Class I (US FDA UDI)

by Tens Plus Industrial Company

Identity

Trade Name
MOXI ROLLS (NY) FDA UDI
Generic Name
Moxa FDA UDI
Model / Reference
Roll.Nien.Y FDA UDI

Identifiers

Primary DI / UDI-DI
14897076722478 FDA UDI
FDA Product Code
IMA FDA UDI
GMDN Term
Moxa FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5730 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Moxa

Moxi Rolls (ny) by Tens Plus Industrial Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Moxa.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 55c22316-9e2b-4fa2-80d8-b0dde6be010a 32 fields · synced Jun 1, 2026